The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126761011 12676101 1 I 20160512 20160823 20160823 PER US-ASTRAZENECA-2016SE52519 ASTRAZENECA 0.00 F Y 77.60000 KG 20160823 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126761011 12676101 1 PS ARIMIDEX ANASTROZOLE 1 Oral 20541 1 MG TABLET QD
126761011 12676101 2 SS ARIMIDEX ANASTROZOLE 1 Oral 20541 1 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126761011 12676101 1 Breast cancer female
126761011 12676101 2 Breast cancer female

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126761011 12676101 Anxiety
126761011 12676101 Arthralgia
126761011 12676101 Asthenia
126761011 12676101 Blood cholesterol increased
126761011 12676101 Depressed mood
126761011 12676101 Depression
126761011 12676101 Dizziness
126761011 12676101 Dyspepsia
126761011 12676101 Fatigue
126761011 12676101 Headache
126761011 12676101 Insomnia
126761011 12676101 Mood altered
126761011 12676101 Nausea
126761011 12676101 Onychoclasis
126761011 12676101 Panic disorder
126761011 12676101 Rash
126761011 12676101 Syncope
126761011 12676101 Temperature intolerance
126761011 12676101 Throat tightness

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126761011 12676101 1 201111 0